JP2005510607A5 - - Google Patents
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- JP2005510607A5 JP2005510607A5 JP2003547500A JP2003547500A JP2005510607A5 JP 2005510607 A5 JP2005510607 A5 JP 2005510607A5 JP 2003547500 A JP2003547500 A JP 2003547500A JP 2003547500 A JP2003547500 A JP 2003547500A JP 2005510607 A5 JP2005510607 A5 JP 2005510607A5
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- Prior art keywords
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- hydrogen
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- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 239000001257 hydrogen Substances 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 239000000758 substrate Substances 0.000 claims 4
- 239000006184 cosolvent Substances 0.000 claims 3
- 239000003085 diluting agent Substances 0.000 claims 3
- 238000010790 dilution Methods 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 2
- 229920001774 Perfluoroether Polymers 0.000 claims 2
- 150000005215 alkyl ethers Chemical class 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 230000001588 bifunctional Effects 0.000 claims 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims 2
- 239000011248 coating agent Substances 0.000 claims 2
- 238000000576 coating method Methods 0.000 claims 2
- 239000012141 concentrate Substances 0.000 claims 2
- 235000008504 concentrate Nutrition 0.000 claims 2
- 239000008240 homogeneous mixture Substances 0.000 claims 2
- -1 hydroxyl hydrogen Chemical compound 0.000 claims 2
- 125000005647 linker group Chemical group 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
- 229920005862 polyol Polymers 0.000 claims 2
- 150000003077 polyols Chemical class 0.000 claims 2
- 235000020354 squash Nutrition 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 239000004721 Polyphenylene oxide Chemical class 0.000 claims 1
- 230000003667 anti-reflective Effects 0.000 claims 1
- 239000003125 aqueous solvent Substances 0.000 claims 1
- 239000000919 ceramic Substances 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 239000011521 glass Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000010702 perfluoropolyether Substances 0.000 claims 1
- 229920000570 polyether Chemical class 0.000 claims 1
- 238000003672 processing method Methods 0.000 claims 1
Claims (5)
Rf 1−[−Q−[SiY3-xR1 x]z]y (I)
{式中、Rf 1は、一官能性又は二官能性フッ素化基を表し、
Qは、独立して、有機二官能性又は三官能性結合基を表し、
R1は、独立して、C1〜C4アルキル基を表し、
Yは、独立して、C1〜C4アルコキシ基、又は構造式−O−A−R3の親水性アルコキシ基を表すが、但し、少なくとも1つのYが前記親水性アルコキシ基であり、式中、各Aは、独立して、a)式、(CHR2−CH2O)q(式中、qは、1〜40の値を有する数であり、R2は、独立して水素又はメチルであり、R2の少なくとも70%は水素である)を有するか、又は(b)1つのOHおよび1つのヒドロキシル水素を除去することにより、ポリオール、又は、そのアルキルエーテル又はポリエーテル誘導体から誘導される、二官能性親水基を含み、
および、式中、R3は独立して、水素、又は炭素原子数1〜4の低級アルキル基であり、
xは、0又は1であり、
yは、1又は2であり、
zは、1又は2である}、および
(b)少なくとも1種類の水と完全に混和性の有機補助溶媒と少なくとも1種類のフッ素化界面活性剤のうちの一方又は両方、
を含む均一な混合物を含む、希釈可能な非水性濃縮物。 (A) at least one self-emulsifying fluorinated alkoxysilane of formula I,
R f 1 - [- Q- [ SiY 3-x R 1 x] z] y (I)
{Wherein R f 1 represents a monofunctional or difunctional fluorinated group;
Q independently represents an organic difunctional or trifunctional linking group;
R 1 independently represents a C 1 -C 4 alkyl group,
Y independently represents a C 1 to C 4 alkoxy group or a hydrophilic alkoxy group of the structural formula —O—A—R 3 , provided that at least one Y is the hydrophilic alkoxy group ; Wherein each A is independently a) a formula, (CHR 2 —CH 2 O) q , wherein q is a number having a value from 1 to 40 and R 2 is independently hydrogen or Or at least 70% of R 2 is hydrogen) or (b) derived from a polyol or its alkyl ether or polyether derivative by removing one OH and one hydroxyl hydrogen Containing a bifunctional hydrophilic group,
In the formula, R 3 is independently hydrogen or a lower alkyl group having 1 to 4 carbon atoms,
x is 0 or 1,
y is 1 or 2,
z is 1 or 2}, and (b) one or both of at least one water fully miscible organic co-solvent and at least one fluorinated surfactant,
A dilutable non-aqueous concentrate comprising a homogeneous mixture comprising
b.i.式Iの少なくとも1種類の自己乳化性フッ素化アルコキシシラン、
Rf 1−[−Q−[SiY3-xR1 x]z]y (I)
{式中、Rf 1は、−(CnF2n)−、−(CnF2nO)−、−(CF(Z))−、−(CF(Z)O)−、−(CF(Z)CnF2nO)−、−(CnF2nCF(Z)O)−およびこれらの組合せからなる群から選択される過フッ素化繰り返し単位を含む、一官能性又は二官能性パーフルオロポリエーテルを表し、式中、Zは、フッ素原子、パーフルオロアルキル基、酸素置換パーフルオロアルキル基、パーフルオロアルコキシ基、および酸素置換パーフルオロアルコキシ基であり、そして、式中、nは1〜6であり、
Qは、独立して、有機二官能性又は三官能性結合基を表し、
R1は、独立して、C1〜C4アルキル基を表し、
Yは、独立して、C1〜C4アルコキシ基、又は構造式−O−A−R3の親水性アルコキシ基を表すが、但し、少なくとも1つの親水性アルコキシ基がフッ素化アルコキシシラン中に存在し、式中、各Aは、独立して、a)式、(CHR2−CH2O)q(式中、qは、1〜40の値を有する数であり、R2は、独立して水素又はメチルであり、R2の少なくとも70%が水素である)を有するか、又は(b)1つのOHおよび1つのヒドロキシル水素を除去することにより、ポリオール、又は、そのアルキルエーテル又はポリエーテル誘導体から誘導される、二官能性親水基を含み、
および、式中、R3は独立して、水素、又は炭素原子数1〜4の低級アルキル基であり、
xは、0又は1であり、
yは、1又は2であり、
zは、1又は2である}、および
ii.少なくとも1種類の水に完全に混和性の有機補助溶媒と少なくとも1種類のフッ素化界面活性剤のうちの一方又は両方、
を含む、均一な混合物を含む希釈可能な非水性濃縮物、
を含む水性希釈液。 a. A dilution medium comprising water or an aqueous solvent mixture comprising water and at least one organic co-solvent; and b. i. At least one self-emulsifying fluorinated alkoxysilane of formula I;
R f 1 - [- Q- [ SiY 3-x R 1 x] z] y (I)
{Wherein, R f 1 is, - (C n F 2n) -, - (C n F 2n O) -, - (CF (Z)) -, - (CF (Z) O) -, - (CF (Z) C n F 2n O ) -, - (C n F 2n CF (Z) O) - is selected from the group consisting of including perfluorinated repeating units, monofunctional or difunctional Represents a perfluoropolyether, wherein Z is a fluorine atom, a perfluoroalkyl group, an oxygen-substituted perfluoroalkyl group, a perfluoroalkoxy group, and an oxygen-substituted perfluoroalkoxy group, and wherein n is 1-6,
Q independently represents an organic difunctional or trifunctional linking group;
R 1 independently represents a C 1 -C 4 alkyl group,
Y independently represents a C 1 to C 4 alkoxy group or a hydrophilic alkoxy group of the structural formula —O—A—R 3 , provided that at least one hydrophilic alkoxy group is present in the fluorinated alkoxysilane. Wherein each A is independently a) a formula, (CHR 2 —CH 2 O) q , where q is a number having a value of 1-40, and R 2 is independently Or at least 70% of R 2 is hydrogen) or (b) by removing one OH and one hydroxyl hydrogen, the polyol or its alkyl ether or poly Containing a bifunctional hydrophilic group derived from an ether derivative;
In the formula, R 3 is independently hydrogen or a lower alkyl group having 1 to 4 carbon atoms,
x is 0 or 1,
y is 1 or 2,
z is 1 or 2}, and ii. One or both of at least one water-miscible organic cosolvent and at least one fluorinated surfactant;
A dilutable non-aqueous concentrate comprising a homogeneous mixture,
An aqueous diluent containing
b.請求項2に記載の水性希釈液を前記基材上に塗付し、前記水性希釈液を硬化させることにより得られる、前記基材上の塗膜、
を含む物品。 a. A substrate, and b. A coating film on the substrate obtained by applying the aqueous diluent according to claim 2 on the substrate and curing the aqueous diluent,
Articles containing.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/994,561 US20030113555A1 (en) | 2001-11-27 | 2001-11-27 | Compositions for aqueous delivery of self-emulsifying fluorinated alkoxysilanes |
PCT/US2002/034280 WO2003046056A1 (en) | 2001-11-27 | 2002-10-25 | Compositions for aqueous delivery of self-emulsifying fluorinated alkoxysilanes |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2005510607A JP2005510607A (en) | 2005-04-21 |
JP2005510607A5 true JP2005510607A5 (en) | 2006-01-05 |
Family
ID=25540801
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2003547500A Pending JP2005510607A (en) | 2001-11-27 | 2002-10-25 | Composition for water-based delivery of self-emulsifying fluorinated alkoxysilanes |
Country Status (7)
Country | Link |
---|---|
US (1) | US20030113555A1 (en) |
EP (1) | EP1448677A1 (en) |
JP (1) | JP2005510607A (en) |
CN (1) | CN1285645C (en) |
AU (1) | AU2002357671A1 (en) |
MX (1) | MXPA04004978A (en) |
WO (1) | WO2003046056A1 (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6861149B2 (en) * | 2001-11-27 | 2005-03-01 | 3M Innovative Properties Company | Compositions for aqueous delivery of self-emulsifying fluorinated alkoxysilanes |
US20040241396A1 (en) * | 2003-05-29 | 2004-12-02 | 3M Innovative Properties Company | Method of modifying a surface of a substrate and articles therefrom |
US20040241323A1 (en) * | 2003-05-29 | 2004-12-02 | 3M Innovative Properties Company | Method for applying adhesive to a substrate |
US20040241395A1 (en) * | 2003-05-29 | 2004-12-02 | 3M Innovative Properties Company | Method of modifying a surface of a substrate and articles therefrom |
US6969166B2 (en) * | 2003-05-29 | 2005-11-29 | 3M Innovative Properties Company | Method for modifying the surface of a substrate |
US7652115B2 (en) * | 2003-09-08 | 2010-01-26 | 3M Innovative Properties Company | Fluorinated polyether isocyanate derived silane compositions |
US7141537B2 (en) * | 2003-10-30 | 2006-11-28 | 3M Innovative Properties Company | Mixture of fluorinated polyethers and use thereof as surfactant |
US7803894B2 (en) * | 2003-12-05 | 2010-09-28 | 3M Innovatie Properties Company | Coating compositions with perfluoropolyetherisocyanate derived silane and alkoxysilanes |
US7321018B2 (en) | 2003-12-23 | 2008-01-22 | 3M Innovative Properties Company | Compositions for aqueous delivery of fluorinated oligomeric silanes |
EP1942225A4 (en) * | 2005-09-21 | 2012-05-30 | Daikin Ind Ltd | Treatment for paper and method for treatment of paper |
US7964552B2 (en) | 2006-12-15 | 2011-06-21 | E. I. Du Pont De Nemours And Company | Fluorosurfactant with disproportionate effect |
US20080146820A1 (en) * | 2006-12-15 | 2008-06-19 | Axel Hans-Joachim Herzog | Phosphate fluorosurfactant and siloxane surfactant |
CN105037412A (en) * | 2007-10-01 | 2015-11-11 | 3M创新有限公司 | Cationic fluorinated ether silane compositions and related methods |
US8501641B2 (en) * | 2007-10-01 | 2013-08-06 | 3M Innovative Properties Company | Compositions comprising cationic fluorinated ether silanes, and related methods |
JPWO2009069183A1 (en) * | 2007-11-30 | 2011-04-07 | 小川 一文 | Humidity control material |
EP2412779A4 (en) * | 2009-03-25 | 2014-01-15 | Daikin Ind Ltd | Surfactant comprising fluorine-containing polymer |
WO2013106383A1 (en) | 2012-01-10 | 2013-07-18 | 3M Innovative Properties Company | Aqueous fluorinated silane dispersions |
WO2014137801A1 (en) * | 2013-03-03 | 2014-09-12 | John Moore | Temporary adhesive with tunable adhesion force sufficient for processing thin solid materials |
KR20200021200A (en) * | 2018-08-20 | 2020-02-28 | 삼성전자주식회사 | Surface coating material and film and stacked structure and display device |
CN115537120B (en) * | 2022-11-03 | 2023-07-21 | 山东省科学院新材料研究所 | Heat-resistant grafted silicone resin coating and preparation method thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU632869B2 (en) * | 1989-12-14 | 1993-01-14 | Minnesota Mining And Manufacturing Company | Fluorocarbon-based coating compositions and articles derived therefrom |
US5702509A (en) * | 1995-12-22 | 1997-12-30 | Minnesota Mining And Manufacturing Company | Masonry treatment composition |
US6277485B1 (en) * | 1998-01-27 | 2001-08-21 | 3M Innovative Properties Company | Antisoiling coatings for antireflective surfaces and methods of preparation |
US6613860B1 (en) * | 2000-10-12 | 2003-09-02 | 3M Innovative Properties Company | Compositions comprising fluorinated polyether silanes for rendering substrates oil and water repellent |
-
2001
- 2001-11-27 US US09/994,561 patent/US20030113555A1/en not_active Abandoned
-
2002
- 2002-10-25 JP JP2003547500A patent/JP2005510607A/en active Pending
- 2002-10-25 EP EP20020792207 patent/EP1448677A1/en not_active Withdrawn
- 2002-10-25 AU AU2002357671A patent/AU2002357671A1/en not_active Abandoned
- 2002-10-25 CN CNB028236106A patent/CN1285645C/en not_active Expired - Fee Related
- 2002-10-25 WO PCT/US2002/034280 patent/WO2003046056A1/en active Application Filing
- 2002-10-25 MX MXPA04004978A patent/MXPA04004978A/en active IP Right Grant
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